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    A homozygous <i>IER3IP1</i> mutation causes microcephaly with simplified gyral pattern, epilepsy, and permanent neonatal diabetes syndrome (MEDS)

    A homozygous <i>IER3IP1</i> mutation causes microcephaly with simplified gyral pattern, epilepsy, and permanent neonatal diabetes syndrome (MEDS) by Ghada M. H. Abdel‐Salam, Ashleigh E. Schaffer, Maha S. Zaki, Tracy Dixon‐Salazar, Inas S. Mostafa, Hanan H. Afifi, Joseph G. Gleeson

    Published 2012
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